Literature DB >> 7476180

Open complex formation by Escherichia coli RNA polymerase: the mechanism of polymerase-induced strand separation of double helical DNA.

P L deHaseth1, J D Helmann.   

Abstract

Escherichia coli RNA polymerase is able to site-specifically melt 12 bp of promoter DNA at temperatures far below those normally associated with DNA melting. Here we consider several models to explain how RNA polymerase destabilizes duplex DNA. One popular model proposes that upon binding to the promoter, RNA polymerase untwists the spacer DNA between the -10 and -35 regions, which results in a destabilization of the -10 region at a TA base step where melting initiates. Promoter untwisting may result, in part, from extensive wrapping of the DNA around RNA polymerase. Formation of the strand-separated open complex appears to be facilitated by specific protein-DNA interactions which occur predominantly on the non-template strand. Recent evidence suggests that these include important contacts with sigma factor region 2.3, which we propose binds the displaced single strand of DNA.

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Year:  1995        PMID: 7476180     DOI: 10.1111/j.1365-2958.1995.tb02309.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  44 in total

1.  Mechanism of repression of the aroP P2 promoter by the TyrR protein of Escherichia coli.

Authors:  J Yang; P Wang; A J Pittard
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Interactions of Escherichia coli sigma(70) within the transcription elongation complex.

Authors:  S S Daube; P H von Hippel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-20       Impact factor: 11.205

3.  Multiple mechanisms of phase variation of PorA in Neisseria meningitidis.

Authors:  A van der Ende; C T Hopman; J Dankert
Journal:  Infect Immun       Date:  2000-12       Impact factor: 3.441

Review 4.  The bacterial enhancer-dependent sigma(54) (sigma(N)) transcription factor.

Authors:  M Buck; M T Gallegos; D J Studholme; Y Guo; J D Gralla
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

5.  Strong minor groove base conservation in sequence logos implies DNA distortion or base flipping during replication and transcription initiation.

Authors:  T D Schneider
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

6.  Structure-based analysis of RNA polymerase function: the largest subunit's rudder contributes critically to elongation complex stability and is not involved in the maintenance of RNA-DNA hybrid length.

Authors:  Konstantin Kuznedelov; Nataliya Korzheva; Arkady Mustaev; Konstantin Severinov
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

7.  In vitro properties of RpoS (sigma(S)) mutants of Escherichia coli with postulated N-terminal subregion 1.1 or C-terminal region 4 deleted.

Authors:  J Gowrishankar; Kaneyoshi Yamamoto; P R Subbarayan; Akira Ishihama
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

8.  Identification and analysis of 'extended -10' promoters in Escherichia coli.

Authors:  Jennie E Mitchell; Dongling Zheng; Stephen J W Busby; Stephen D Minchin
Journal:  Nucleic Acids Res       Date:  2003-08-15       Impact factor: 16.971

9.  Cold shock induction of the cspL gene in Lactobacillus plantarum involves transcriptional regulation.

Authors:  Sylviane Derzelle; Bernard Hallet; Thierry Ferain; Jean Delcour; Pascal Hols
Journal:  J Bacteriol       Date:  2002-10       Impact factor: 3.490

10.  The strong efficiency of the Escherichia coli gapA P1 promoter depends on a complex combination of functional determinants.

Authors:  Benoit Thouvenot; Bruno Charpentier; Christiane Branlant
Journal:  Biochem J       Date:  2004-10-15       Impact factor: 3.857

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